Label: ISOPROPYL RUBBING ALCOHOL 99%- isopropyl alcohol liquid
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NDC Code(s):
52000-049-01,
52000-049-02,
52000-049-03,
52000-049-04, view more52000-049-05, 52000-049-06, 52000-049-07
- Packager: Universal Distribution Center LLC
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 20, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- SPL UNCLASSIFIED SECTION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ISOPROPYL RUBBING ALCOHOL 99%
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52000-049 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 99 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52000-049-01 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/20/2020 2 NDC:52000-049-02 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/20/2020 3 NDC:52000-049-03 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/20/2020 4 NDC:52000-049-04 296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/20/2020 5 NDC:52000-049-05 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/20/2020 6 NDC:52000-049-06 414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/20/2020 7 NDC:52000-049-07 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/20/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/20/2020 Labeler - Universal Distribution Center LLC (019180459) Registrant - Jell Pharmaceuticals Pvt. Ltd. (726025211) Establishment Name Address ID/FEI Business Operations Jell Pharmaceuticals Pvt. Ltd. 726025211 manufacture(52000-049)